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“Safety by Design” for Better NDA, ANDA + OTC Applications

Colorcon Inc. | 19-Sep-2016 | PDF Technical / white paper
Review a new Colorcon Technical Paper offering a concise summary of key points covered in the recent US Center for Drug Evaluation and Re...
SGS-LSS

Amino Acid Analysis of Pharmaceutical Products

SGS | 11-Jul-2016 | PDF Technical / white paper
Amino Acid Analysis in general can be used for identification testing of biopharmaceutical active ingredients and the determination of im...

Rapid Microbiological Method Statistics & Validation

EMD Millipore | 17-May-2016 | Webinar On-Demand Supplier Webinar
It is well known that implementation of Rapid Microbiological Methods in Pharma environments is accompanied by a large validation workloa...

Free On-Demand Webinar: Overcoming Your Rapid Microbial Method Validation Challenges.

EMD Millipore | 03-Dec-2015 | Webinar On-Demand Supplier Webinar
Merck Millipore, Life Science subsidiary of Merck, Darmstadt, Germany, invites you to join a free, on-demand webinar on ways to overcome...

Live Webinar on Recent PAT applications for Softgels presented by Softigel by Procaps

Procaps S.A. | 30-Nov-2015 | Webinar On-Demand Supplier Webinar
Process Analytical Technologies (PAT) in solid dosages forms are commonly used for tablets. Procaps brings to you this webinar inten...
Live webinar on disinfection processes & sampling on sanitized surfaces

Live webinar on disinfection processes & sampling on sanitized surfaces

EMD Millipore | 22-Oct-2015 | Webinar On-Demand Supplier Webinar
This webinar will inform about the Disinfection management in pharmaceutical cleanrooms. The guest speaker Tim Sandle will talk about reg...

Product Development Using the NDA 505(b)(2) Approval Pathway

Capsugel | 29-Sep-2015 | Webinar On-Demand Supplier Webinar
The 505(b)(2) NDA pathway is increasingly utilized to bring improved and differentiated products to market faster and more cost effective...

Article on Viral Clearance for Biopharmaceuticals

Catalent | 24-Aug-2015 | PDF Technical / white paper
Viral clearance studies are mandated prior to entering clinical trials and for commercial launch of biopharmaceuticals.  These studi...
How BASF supports its pharmaceutical customers towards compliance

ICH Q3D Guideline for Elemental Impurities – How BASF supports its pharmaceutical customers towards compliance

BASF SE | 14-Apr-2015 | Webinar On-Demand Supplier Webinar
On December 19, 2014, the Guideline "ICH Q3D - Elemental Impurities" was issued by the ICH, providing a global policy for limi...
The in-PharmaTechnologist Anti-counterfeiting Forum

The in-PharmaTechnologist Anti-counterfeiting Forum

William Reed Business Media | 16-Apr-2015 | Webinar On-Demand Supplier Webinar
Drug counterfeiting: a pharmaceutical industry problemCounterfeiters rely on two things: poorly secured pharmaceutical supply chains; and...
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